Evaluation and application of anion exchange resins to measure groundwater uranium flux at a former uranium mill site

被引:33
作者
Stucker, Valerie [1 ]
Ranville, James [1 ]
Newman, Mark [2 ]
Peacock, Aaron [4 ]
Cho, Jaehyun [3 ]
Hatfield, Kirk [2 ]
机构
[1] Colorado Sch Mines, Dept Chem & Geochem, Golden, CO 80401 USA
[2] Univ Florida, Dept Civil & Coastal Engn, Gainesville, FL USA
[3] Univ Florida, Dept Environm Engn Sci, Gainesville, FL 32611 USA
[4] Microbial Insights Inc, Rockford, TN USA
关键词
Ion exchange; Contaminant; Passive flux meter; Sorption; SORPTION BEHAVIOR; ION-EXCHANGE; CONTAMINATED GROUNDWATER; POROUS-MEDIA; REMOVAL; WATER; POLY(4-VINYLPYRIDINE); SULFATE; METER;
D O I
10.1016/j.watres.2011.06.030
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Laboratory tests and a field validation experiment were performed to evaluate anion exchange resins for uranium sorption and desorption in order to develop a uranium passive flux meter (PFM). The mass of uranium sorbed to the resin and corresponding masses of alcohol tracers eluted over the duration of groundwater installation are then used to determine the groundwater and uranium contaminant fluxes. Laboratory based batch experiments were performed using Purolite A500, Dowex 21K and 21K XLT, Lewatit S6328 A resins and silver impregnated activated carbon to examine uranium sorption and extraction for each material. The Dowex resins had the highest uranium sorption, followed by Lewatit, Purolite and the activated carbon. Recoveries from all ion exchange resins were in the range of 94-99% for aqueous uranium in the environmentally relevant concentration range studied (0.01-200 ppb). Due to the lower price and well-characterized tracer capacity, Lewatit S6328 A was used for field-testing of PFMs at the DOE UMTRA site in Rifle, CO. The effect on the flux measurements of extractant (nitric acid)/resin ratio, and uranium loading were investigated. Higher cumulative uranium fluxes (as seen with concentrations > 1 ug U/gram resin) yielded more homogeneous resin samples versus lower cumulative fluxes (<1 ug U/gram resin), which caused the PFM to have areas of localized concentration of uranium. Resin homogenization and larger volume extractions yield reproducible results for all levels of uranium fluxes. Although PFM design can be improved to measure flux and groundwater flow direction, the current methodology can be applied to uranium transport studies. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:4866 / 4876
页数:11
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